A method is disclosed for producing an agglomerated molybdenum plasma spray powder with a controlled level of oxygen which comprises forming a relatively uniform mixture of agglomerated powders containing molybdenum dioxide and one or more ammonium-containing compounds of molybdenum wherein the mixture has an oxygen content of greater than about 25% by weight and reducing the mixture in a moving bed furnace at a temperature of from about 700°C to about 1000°C for a sufficient time to remove a portion of the oxygen therefrom and form reduced molybdenum powder agglomerates having an oxygen content of no greater than about 25% by weight. The reduction takes place in the direction from the outside surface of the agglometates to the inside surface.

Patent
   5173108
Priority
Mar 21 1989
Filed
Nov 12 1991
Issued
Dec 22 1992
Expiry
Dec 22 2009
Assg.orig
Entity
Large
11
15
all paid
1. A method of producing an agglomerated molybdenum plasma spray powder with a controlled level of oxygen, said method comprising:
a) milling molybdenum dioxide powder to a particle size less than about 10 micrometers;
b) forming a slurry consisting of said milled molybdenum dioxide powder and ammonium paramolybdate crystals dissolved in water;
c) forming a uniform mixture of agglomerated powders consisting of molybdenum dioxide and ammonium paramolybdate by drying said slurry, wherein the mixture has an oxygen content of greater than about 25% by weight; and
d) reducing said mixture in a rotating bed furnace in a hydrogen atmosphere at a temperature of from about 700°C to about 1000°C for a sufficient time to remove a portion of the oxygen therefrom and form reduced molybdenum powder agglomerates having an oxygen content of from about 7% to about 10% by weight.

This is a continuation of copending application Ser. No. 07/515,535, filed on Apr. 13, 1990, now abandoned which is a continuation of copending application Ser. No. 07/326,826, filed on Mar. 21, 1989, now abandoned.

This invention is related to application 07/326,827, filed Mar. 21, 1989, now abandoned, entitled "Method For Controlling The Oxygen Content In Agglomerated Molybdenum Powders", which is filed concurrently herewith.

This invention relates to a method for controlling the oxygen content of agglomerated molybdenum-containing powders by controlled reduction thereof. More particularly it relates to a method of introducing a controlled amount of oxygen into agglomerated molybdenum-containing powders by reducing powders of molybdenum dioxide and one or more ammonium-containing compounds of molybdenum.

Flame spraying and plasma spraying are common techniques for the application of protective and wear resistant coatings of various metals, ceramics, and cermets, usually to metal surfaces (substrates). Flame spraying is commonly used to produce molybdenum-containing coatings on piston rings for internal combustion automobile engines and synchronizer rings for manual transmissions for automobiles and trucks.

An electric arc or flame can be used to melt the end of a continuously fed coil of molybdenum wire as a gas propels the molten droplets which form onto a substrate for example, the wear surface of a cast iron piston ring where it splats and solidifies, forming the coating in successive layers. Because of the presence of excess oxygen either from the flame or the surrounding air, or both, the coatings produced by this technique contain large quantities of oxygen, typically from about 7% to about 8% in solution and as various molybdenum oxides. The large quantities of oxygen in the molybdenum harden the coating.

In the plasma spraying of molybdenum, there is usually a minimum of oxygen in the sprayed coating due to the use of an oxygen-lean plasma gas system. That is, argon, helium, hydrogen, nitrogen, or combinations of these gases, all of which are relatively free from oxygen, are used in the plasma spraying process. Hence, any oxygen in the sprayed coating is due to oxidation of the molten particles caused by oxygen from the surrounding air mixing with the plasma gas and/or surface oxidation of the freshly deposited coating. In such "pure" molybdenum coatings the oxygen level is in the 1% to 2% range. Such coatings are softer than their flame sprayed counterparts.

For higher hardness, therefore, a more expensive process such as the flame spray process which requires wire, or a more expensive powder such as molybdenum plus nickel-base alloy must be used.

It would be desirable therefore to have a method of producing molybdneum powders of sufficiently high oxygen content to enable them to be used in a plasma spray process to produce hard coatings.

U.S. Pat. No. 4,624,700 relates to a method to control the oxygen content of agglomerated molybdenum powders by controlled reduction of the powders. This is done by reducing a mixture of molybdenum and one or more oxygen containing compounds of molybdenum under controlled conditions. The mixture is made up of molybdenum and typically mixtures of compounds such as molybdenum dioxide, molybdenum trioxide and ammonium paramolybdate.

U.S. Pat. No. 4,146,400 relates to a method for introducing a controlled level of oxygen into an agglomerated molybdenum metal powder involving heating the powder at a sufficient temperature for a sufficient time in the presence of water vapor and a non-oxidizing atmosphere with the amount of non-oxidizing atmosphere being controlled to produce a partially-oxidized molybdenum powder.

U.S. Pat. No. 4,146,388 describes and claims molybdenum plasma spray powders and a process for producing the powders of molybdenum and oxides of molybdenum having an oxygen content of from about 0.5 to about 15% by weight oxygen. The process involves passing molybdenum particles through a plasma with oxygen or oxides of molybdenum to produce the oxidized powder.

In accordance with one aspect of this invention, there is provided a method for producing an agglomerated molybdenum plasma spray powder with a controlled level of oxygen which comprises forming a relatively uniform mixture of agglomerated powders containing molybdenum dioxide and one or more ammonium-containing compounds of molybdenum wherein the mixture has an oxygen content of greater than about 25% by weight and reducing the mixture in a moving bed furnace at a temperature of from about 700° C. to about 1000°C for a sufficient time to remove a portion of the oxygen therefrom and form reduced molybdenum powder agglomerates having an oxygen content of no greater than about 25% by weight. The reduction proceeds in the direction from the outside surface of the agglomerates to the inside surface.

For a better understanding of the present invention, together with other and further objects, advantages and capabilities thereof, reference is made to the following disclosure and appended claims in connection with the above description of some of the aspects of the invention.

In the particular applications in which the controlled oxygen molybdenum powders resulting from the method of this invention are preferably used, that is, in plasma spray applications to produce plasma spray coatings, the desired oxygen content is typically no greater than about 10% and most preferably from about 7% to about 10% by weight. At levels lower than this, the hardness and wear resistance of the plasma sprayed coating is not sufficiently improved. At levels higher than this range, the coating integrity or bond strength is compromised.

According to the present invention the mixture consists essentially of molybdenum dioxide, and one or more ammonium-containing compounds of molybdenum. The ammonium-containing compounds of molybdenum are normally ammonium paramolybdate, ammonium dimolybdate and combinations of these. Most preferred is ammonium paramolybdate.

It is to be understood that any mixture of molybdenum dioxide and ammonium-containing compounds can be used as long as the oxygen content of the agglomerated mixture is greater than about 25% by weight.

The mixture can be agglomerated by any of several methods well known in the art.

One preferred method of agglomerating the powders involves generally forming a slurry of water, ammonia or ammonium hydroxide, molybdenum trioxide, and molybdenum dioxide particles. Ammonium paramolybdate is formed from the molybdenum trioxide and ammonium hydroxide and acts as the binder in this system. The resulting slurry is then spray dried to remove the water and form the relatively uniform agglomerated mixture which consists of essentially spherical particles. The above method of forming the agglomerated mixture is described in U.S. Pat. No. 3,973,948 which is hereby incorporated by reference.

Another method of forming the relatively uniform agglomertated mixture is by first forming a slurry as described above. The water is allowed to evaporate while the slurry is being continually stirred to break up the material. The resultant coarse moist powder is then forced through a 100 mesh screen and collected. The powder is then further dried with gentle agitation. The final agglomerated mixture is then screened from this dried mixture.

As an alternative to forming the ammonium paramolybdate (APM) in the slurry, commercially available APM crystals can be dissolved in the water to be used to form the slurry.

Some preferred methods of agglomerating the molybdenum powder are disclosed also in a paper entitled "Properties of Oxygen Bearing Molybdenum Coatings," published in the proceedings of the Ninth International Thermal Spray Conference, Denhaag, Netherlands, May 19-23, 1980.

The resulting agglomerated mixture is then reduced at a temperature of from about 700°C to about 1000°C for a sufficient time to remove a portion of the oxygen and form a molybdenum powder having an oxygen content of no greater than about 25% and preferably from about 7% to about 10% by weight.

The reduction is done in a dry hydrogen atmosphere in standard moving bed type furnace such as a fluidized bed or rotary furnace. The time depends on the temperature and on the nature of the equipment. However, typical times are from about 2 hours to about 4 hours. The reducing conditions are adjusted to give the final desired oxygen content. The advantages of using a fluidized bed or rotary calciner in the method of the present invention over static bed reduction are that a bed depth problem is avoided resulting in a more uniform reduction than in the static bed furnace. In a fluidized bed or rotary calciner the reduction of the agglomerates takes place from the outside of the agglomerates to the inside resulting in the metal phase being on the outside of the agglomerates. This results in a more efficient melting of the agglomerates in the plasma application and therefore produces a coating with better bonding charactristics.

The resulting powders with controlled oxygen levels are used in plasma spraying applications to produce coatings such as on synchronizer rings and piston rings.

To more fully illustrate this invention, the following non-limiting example is presented. All parts, portions, and percentages are on a weight basis unless otherwise stated.

An aqueous slurry is made up consisting essentially of about 85% solids, the solids consisting essentially of molybdenum dioxide. The slurry containing the molybdenum dioxide is milled in a conventional attritor mill to ensure that the molybdenum dioxide particles are all less than about 10 micrometers in diameter. Ammonium paramolybdate crystals are then added to the slurry. The APM crystals are added to the slurry in a ratio of about 4.5 pounds of APM per gallon of water. The ratio is slightly less than the maximum solubility limit of APM in water. The slurry is dried in a conventional spray dryer to produce relatively uniform agglomerated mixture consisting of particles which are essentially spherical in shape. The mixture is reduced in dry hydrogen at about 800°C for about 2 hours resulting in a free-flowing molybdenum spray powder having an oxygen content of from about 7% to about 8%.

While there has been shown and described what are at present considered the preferred embodiments of the invention, it will be obvious to those skilled in the art that various changes and modifications may be made therein without departing from the scope of the invention as defined by the appended claims.

Houck, David L.

Patent Priority Assignee Title
5439638, Jul 16 1993 CYTOSORBENTS CORPORATION Method of making flowable tungsten/copper composite powder
5897962, Jul 16 1993 GLOBAL TUNGSTEN, LLC; GLOBAL TUNGSTEN & POWDERS CORP Method of making flowable tungsten/copper composite powder
6022395, Mar 24 1998 GLOBAL TUNGSTEN, LLC; GLOBAL TUNGSTEN & POWDERS CORP Method for increasing tap density of molybdenum powder
6551377, Mar 19 2001 RHENIUM ALLOYS, INC Spherical rhenium powder
7470307, Mar 29 2005 Cyprus Amax Minerals Company Metal powders and methods for producing the same
7824465, Mar 29 2005 Cyprus Amax Minerals Company Methods for producing metal powders
8043405, Oct 21 2004 Cyprus Amax Minerals Company Densified molybdenum metal powder
8043406, Oct 21 2004 Cyprus Amax Minerals Company Molybdenum metal powder
8147586, Oct 21 2004 Cyprus Amax Minerals Company Method for producing molybdenum metal powder
8197885, Jan 11 2008 Cyprus Amax Minerals Company Methods for producing sodium/molybdenum power compacts
8206485, Mar 29 2005 Cyprus Amax Minerals Company Metal powders and methods for producing the same
Patent Priority Assignee Title
3973948, Nov 12 1973 GTE Sylvania Incorporated Free flowing powder and process for producing it
4146388, Dec 08 1977 GTE Sylvania Incorporated Molybdenum plasma spray powder, process for producing said powder, and coatings made therefrom
4390368, Apr 01 1981 GTE Products Corporation Flame spray powder
4395279, Nov 27 1981 GTE Products Corporation Plasma spray powder
4502885, Apr 09 1984 GTE Products Corporation Method for making metal powder
4508788, Sep 09 1982 GTE Products Corporation Plasma spray powder
4595412, Jul 22 1985 GTE Products Corporation Production of molybdenum metal
4624700, Feb 20 1986 GTE Products Corporation Method for controlling the oxygen content in agglomerated molybdenum powders
4705560, Oct 14 1986 GTE Products Corporation Process for producing metallic powders
4711661, Sep 08 1986 GTE Products Corporation Spherical copper based powder particles and process for producing same
4773928, Aug 03 1987 GTE Products Corporation Plasma spray powders and process for producing same
4783214, Feb 29 1988 GTE Products Corporation Low oxygen content fine shperical particles and process for producing same by fluid energy milling and high temperature processing
4783218, Sep 08 1986 GTE Products Corporation Process for producing spherical refractory metal based powder particles
CA561559,
EP292798,
////
Executed onAssignorAssigneeConveyanceFrameReelDoc
Nov 12 1991GTE Products Corporation(assignment on the face of the patent)
Jul 31 2008Osram Sylvania, IncGLOBAL TUNGSTEN, LLCASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0217440231 pdf
Jul 31 2008OSRAM SYLVANIA IncGLOBAL TUNGSTEN & POWDERS CORP ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0217440744 pdf
Jul 31 2008GLOBAL TUNGSTEN, LLCGLOBAL TUNGSTEN & POWDERS CORP MERGER SEE DOCUMENT FOR DETAILS 0217630241 pdf
Date Maintenance Fee Events
Mar 18 1996M183: Payment of Maintenance Fee, 4th Year, Large Entity.
Mar 29 1996ASPN: Payor Number Assigned.
Mar 13 2000M184: Payment of Maintenance Fee, 8th Year, Large Entity.
Mar 16 2004M1553: Payment of Maintenance Fee, 12th Year, Large Entity.
Dec 19 2008ASPN: Payor Number Assigned.
Dec 19 2008RMPN: Payer Number De-assigned.


Date Maintenance Schedule
Dec 22 19954 years fee payment window open
Jun 22 19966 months grace period start (w surcharge)
Dec 22 1996patent expiry (for year 4)
Dec 22 19982 years to revive unintentionally abandoned end. (for year 4)
Dec 22 19998 years fee payment window open
Jun 22 20006 months grace period start (w surcharge)
Dec 22 2000patent expiry (for year 8)
Dec 22 20022 years to revive unintentionally abandoned end. (for year 8)
Dec 22 200312 years fee payment window open
Jun 22 20046 months grace period start (w surcharge)
Dec 22 2004patent expiry (for year 12)
Dec 22 20062 years to revive unintentionally abandoned end. (for year 12)